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62 Cards in this Set
- Front
- Back
Refers to the multiplication of a microbe in a host and in the process produces inflammation. |
Infection |
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Any change from the general state of good health. |
Disease |
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Difference between indigneous and transient microbiota |
Indigenous establish themselves in particluar areas, transient come and go |
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Relationship between body and its microbiota |
Symbiosis |
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Microbe benefits, host is unaffected |
commensalism |
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Pathogen causes damage to the host and disease can result |
Parasitism |
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Ability of microorganism to gain entry to the host's tissues and bring about physiological or anatomical changes resulting in altered health and leading to disease. |
Pathogenicity |
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The degree of pathogenicity is called ________. |
Virulence; If disease is going to be mild or severe, it depends on virulence. Ex ebola is more virulent than chicken pox |
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Gene clusters responsible for virulence |
pathogenicity islands |
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exogenouse infection |
pathogen came from outside of the host (air, surface, etc.) |
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endogenous infection |
when normal microbiota causes disease. Ex: woman uses antibiotic, yeast is no longer in check, gains infection |
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Opportunistic Infection |
When commensal microbe takes advantage of a change in the body environment. IE you are immunosuppressed. |
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Infection can be ____________ or ______________. EIther occurs in a healthy person or the latter develops in an individual weakened already. |
Primary;secondary |
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A disease restricted to a single area is called? |
Local |
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A disease that has spread via the blood to deeper organs and systems is called? |
Systemic |
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An infection ending in "emia" means the infection is seen where? |
In the blood |
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Incubation period def: |
Time between entry of host and symptoms |
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Prodromal phase includes: |
Signs and symptoms |
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The stage when signs and symptoms are of greatest intensity; ??Usually when a secondary attack occurs |
Acute or Acme period |
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As the signs and symptoms subside, the host enter _____________________ . |
Period of decline |
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The final stage in which the body's systems return to normal |
Period of convalescence |
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A disease that is short in duration (comes on quick but leaves quick) |
acute disease |
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A disease that lingers for long periods of time |
Chronic |
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List the series of stages of disease progession |
1. Incubation Period 2. Prodromal phase (S&S) 3. Acute or Acme phase (climax of symptoms) 4. Decline phase (s&s fade) 5. Convalscence (body returns to normal) |
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Route by which exogenous pathogen enter the host |
Portal of entry |
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Give examples of portal of entry |
1. respiratory 2. gastrointestinal via fecal-oral 3. sexually transmitted 4. parenteral (piercing skin) |
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number of pathogens needed to cause infection |
Infectious Dose |
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Cell surface components that are "sticky" |
Adhesin |
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True or False: Adhesins create specificity for bacteria; allowing them to adhere to specific tissues. |
True: An exampled is C Diff which uses pili to attached to specific receptor sites . This is why certain bacteria are found to enter in specific portals |
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Define Signs and Symptoms |
Signs are measurable such as a temperature. Symptoms are feelings such as pain |
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The ability to penetrate and spread is called... |
invasiveness |
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Why are some microbes able to go undetected? |
Capsule. ALso, they may evade lysosomes using them to travel into the body. |
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What are examples of virulence factors: |
1. Enzymes 2. Toxins |
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Example of enzyme used by invading microbe and how it works: |
1. Staph produces coagulase; protecting itself from phagocytosis 2. Streptokinase is used to build a clot, hide, then break free 3. Hyuluronidase - enhances pentration through tissues/junctions 4. Leukocidins - cidal + leuko kills wbcs 5. Hemolysins - kills rbcs
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How does a biofilm enhance virulence? |
It can resist body defenses and drugs. WBCs have difficulty reaching bacteria that has enclosed itself in tissue. They do not need to divide under the biofilm therefore drugs that prevent binary fission will not work. |
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The ability of a pathogen to produce toxins |
toxigencity |
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What are the two types of toxins? |
Exotoxin and Endotoxin |
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Difference between exotoxin and endotoxin |
Exo is released from the cell, is made of protein and is heat labile. Specific effects in host. Toxoids can be made.
Endo is part of the cell, produced only by gram neg, made of lipopolysach and is heat stable. Diverse effects in host. Toxoids cannot be made
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Toxins that have been inactivated and can be used in a vaccine. (Toxicity destroyed but still elicits immune reponse). |
Toxoids |
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This toxin interferes with nerve transmission |
Neurotoxin |
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This toxin effects the intestinal tract |
Enterotoxin |
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These toxins function by activating a blood-clotting factor to initiate blood coagulation. Fever appears. |
Endotoxin |
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During bacterial metabolism, this toxin exits the microbe. |
exotoxin |
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These are produced by the host body and neutralize toxins |
antitoxin |
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A disease spread from animal to human |
Zoonosis |
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The place in the environment where a pathogen can be found |
Reservoir |
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Disease cannot be transferred from human to when they are a ______ ________ _______. |
Dead end host |
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Have recovered from the disease but continue to shed disease agents |
carriers |
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Direct ways disease is transmitted. |
1. horizontal 2. respiratory droplets 3. vertical |
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Indirect ways disease is transmitted. |
1. Fomites 2. Vehicle transmission (caca in the agua) 3. Vectors 4. aerosols |
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Difference between mechanical and biolgical vectors |
Mechanical - passively transports microbes on their legs (fly)
Biological - pathogens multiplies in insect before it can infect host (tick) |
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Disease present at a low level in specific geographic area. |
Endemic (endogenous to a spec region) |
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Disease spikes more than expected in a population |
Epidemic (epic) |
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If an abnormally high number of a disease breaks out in one city it is considered an.... |
outbreak |
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worldwide epidemic |
pandemic |
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Disorder acquired during an individual's stay at a hospital or chronic care facility. |
Nosocomial infecion |
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HAIs involve three elements: |
compromised host
source of hospital pathogen
chain of transmission |
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_________________ is thekey to reducing nosocomial infections |
chain of transmission |
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Many nosocomial infections are cause by _______________ agents, microbes that do not normaly cause illness in healthy individuals. |
Opportunistic |
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disease that was previously controlled or on the decline but shows up again |
reemerging (or resurgent) |
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Reemergence is caused by: |
1. changes in land use (contact with animals) 2. Changes in demographic 3. COntaminated food 4. International travel 5. Climate change |
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scientif and med study of causes transmissiona and preventionof a disease in population |
epidemiology |